Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20684520-20684605 | Common:1; Rare:17; Clinvar (benign):1 | ||||
chr14:21511257-21511553 | Rare:86 | ||||
chr14:22766518-22766757 | Common:1; Rare:136 | ||||
chr14:22876714-22877001 | Common:2; Rare:80 | ||||
chr14:22982493-22982739 | Common:1; Rare:93 | ||||
chr14:23095441-23095584 | Common:2; Rare:59 | ||||
chr14:23953730-23953832 | Common:4; Rare:35 | ||||
chr14:24146573-24146741 | Rare:58 | ||||
chr14:24195403-24195781 | Common:1; Rare:90 | ||||
chr14:24232321-24232480 | Common:6; Rare:39 | ||||
chr14:24429810-24430003 | Common:2; Rare:47 | ||||
chr14:24442659-24443043 | Common:5; Rare:121 | ||||
chr14:30622190-30622351 | Rare:58 | ||||
chr14:34982501-34982682 | Common:1; Rare:75 | ||||
chr14:35122217-35122564 | Common:1; Rare:99 |